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1.
During CREAMS expeditions, fCO2 for surface waters was measured continuously along the cruise tracks. The fCO2 in surface waters in summer varied in the range 320–440 μatm, showing moderate supersaturation with respect to atmospheric CO2. In winter, however, fCO2 showed under-saturation of CO2 in most of the area, while varying in a much wider range from 180 to 520 μatm. Some very high fCO2 values observed in the northern East Sea (Japan Sea) appeared to be associated with the intensive convection system developed in the area. A gas-exchange model was developed for describing the annual variation of fCO2 and for estimating the annual flux of CO2 at the air-sea interface. The model incorporated annual variations in SST, the thickness of the mixed layer, gas exchange associated with wind velocity, biological activity and atmospheric concentration of CO2. The model shows that the East Sea releases CO2 into the atmosphere from June to September, and absorbs CO2 during the rest of the year, from October through May. The net annual CO2 flux at the air-sea interface was estimated to be 0.032 (±0.012) Gt-C per year from the atmosphere into the East Sea. Water column chemistry shows penetration of CO2 into the whole water column, supporting a short turnover time for deep waters in the East Sea. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

2.
Fugacity of CO2 (fCO2), temperature, salinity, nutrients, and chlorophyll-a were measured in the surface waters of southwestern East Sea/Japan Sea in July 2005. Surface waters were divided into three waters based on hydrographic characteristics: the water with moderate sea surface temperature (SST) and high sea surface salinity (SSS) located east of the front (East water); the water with high SST and moderate SSS located west of the front (West water); and the water with low SST and SSS located in the middle part of the study area (Middle water). High fCO2 larger than 420 μatm were found in the West water. In the Middle water, CO2 was undersaturated with respect to the atmosphere, with values between 246 and 380 μatm. Moderate fCO2 values ranging from 370 to 420 μatm were observed in the East water. For the East and West waters, estimates of temperature dependency of fCO2 (12.6 and 15.1 μatm °C−1, respectively) were rather similar to a theoretical value, indicating that SST is likely to be a major factor controlling the surface fCO2 distribution in these two regions. In the Middle water, however, the estimated temperature dependence was somewhat lower than the theoretical value, and relatively high concentrations of surface chlorophyll-a coincided with the low surface fCO2, implying that biological uptake may considerably affect the fCO2 distribution. The net sea-to-air CO2 flux of the study area was estimated to be 0.30±4.81 mmol m−2 day−1 in summer, 2005.  相似文献   

3.
The annual cycle of dissolved nutrients and the fugacity of CO2 (fCO2), calculated from the concentration of dissolved inorganic carbon (DIC) and pH, was studied over a 14-month long period (December 1993 to February 1995) at a site in Prydz Bay near Davis Station, Vestfold Hills, East Antarctica. Significant spring decreases in fCO2 began under the sea-ice in mid-October, when both water column and sea-ice algal activity resulted in the removal of nutrients and DIC and increased pH. Minimum fCO2 (<100 μatm) and lowest nutrient and DIC concentrations occurred in December and January. The low summer fCO2 values were clearly the result of biological activity. The seasonal depletion of dissolved nitrate reached 85% in mid-summer when chlorophyll-a concentrations exceeded 15 mg m−3. Oceanic uptake of carbon dioxide from the atmosphere, calculated from the fugacity difference and daily wind speeds, averaged more than 30 mmol m−2 day−1 during the summer ice-free period. This exchange replaced approximately half of the DIC consumed by biological activity. Apparent nutrient utilisation ratios (C/N/P) were close to Redfield values. In autumn fCO2 began to rise, continuing slowly well into winter, and reaching a maximum close to modern atmospheric values between July and September. This increase can be attributed to a combination of local remineralisation of organic carbon in the water column and the steady increase in the mixing depth of the water column. At first glance, this suggests that air–sea equilibration occurred in winter despite the sea-ice cover, perhaps by horizontal circulation from regions outside the pack ice, or through openings in the ice. However, the persistent 15 to 20% undersaturation of dissolved oxygen throughout the winter suggests an alternate explanation. The late winter fCO2 level may represent a characteristic established by global circulation, so that as a result of increasing atmospheric CO2 concentrations, these Antarctic waters are in transition from being a winter-time source of CO2 to the atmosphere to becoming a sink. Our fCO2 observations emphasize the need to address seasonal variations in assessing Antarctic contributions to the oceanic control of atmospheric CO2.  相似文献   

4.
We report several biogeochemical parameters (dissolved inorganic carbon (DIC), total alkalinity (TA), dissolved oxygen (DO), phosphate (PO4), nitrate + nitrite (NO3 + NO2), silicate (Si(OH)4)) in a region off Otaru coast in Hokkaido, Japan on a “weekly” basis during the period of April 2002–May 2003. To better understand the long-term temporal variations of the main factors affecting CO2 flux in this coastal region and its role as a sink/source of atmospheric CO2, we constructed an algorithm of DIC and TA using other hydrographic properties. We estimated the CO2 flux across the air–sea interface by using the classical bulk method. During 1998–2003 in our study region, the estimated fCO2sea ranged about 185–335 μatm. The maximum of fCO2sea in the summer was primarily due to the change of water temperature. The minimum of fCO2sea in the early spring can be explained not only by the change of water temperature but also the change of nutrients and chlorophyll-a. To clarify the factors affecting fCO2sea (water temperature, salinity, and biological activity), we carried out a sensitivity analysis of these effects on the variation of fCO2sea. In spring, the biological effect had the largest effect for the minimum of fCO2sea (40%). In summer, the water temperature effect had the largest effect for the maximum of fCO2sea (25%). In fall, the water temperature effect had the largest effect for the minimum of fCO2sea (53%). In winter, the biological effect had the largest effect for the minimum of fCO2sea (35%).We found that our study region was a sink region of CO2 throughout a year (−0.78 mol/m2/yr). Furthermore, we estimated that the increase of fCO2sea was about 0.56 μatm/yr under equilibrium with the atmospheric CO2 content for the period 1998–2003, with the temporal changes in the variables (T, S, PO4) on fCO2sea, thus as the maximum trend of each variable on fCO2sea was 0.22 μatm/yr, and the trend of residual fCO2 including gas exchange was 0.34 μatm/yr. This result suggests that interaction among variables would affect gas exchange between air and sea effects on fCO2sea. We conclude that this study region as a representative coastal region of marginal seas of the North Pacific is special because it was measured, but there is no particular significance in comparison to any other area.  相似文献   

5.
Coastal upwelling systems are regions with highly variable physical processes and very high rates of primary production and very little is known about the effect of these factors on the short-term variations of CO2 fugacity in seawater (fCO2w). This paper presents the effect of short-term variability (<1 week) of upwelling–downwelling events on CO2 fugacity in seawater (fCO2w), oxygen, temperature and salinity fields in the Ría de Vigo (a coastal upwelling ecosystem). The magnitude of fCO2w values is physically and biologically modulated and ranges from 285 μatm in July to 615 μatm in October. There is a sharp gradient in fCO2w between the inner and the outer zone of the Ría during almost all the sampling dates, with a landward increase in fCO2w.CO2 fluxes calculated from local wind speed and air–sea fCO2 differences indicate that the inner zone is a sink for atmospheric CO2 in December only (−0.30 mmol m−2 day−1). The middle zone absorbs CO2 in December and July (−0.05 and −0.27 mmol·m−2 day−1, respectively). The oceanic zone only emits CO2 in October (0.36 mmol·m−2 day−1) and absorbs at the highest rate in December (−1.53 mmol·m−2 day−1).  相似文献   

6.
In order to construct monthly fields of sea surface fugacity of carbon dioxide (fCO2) on a large scale in the Indian Ocean, we use a one-dimensional model which takes into account the main physical and biogeochemical processes controlling fCO2 variations in the ocean. Physical and biogeochemical processes are constrained by the monthly variations of sea surface temperature, salinity, chlorophyll concentration, wind speed and mixed-layer depth. The model is applied to four locations in the Indian Ocean and it well predicts observed temporal variations in fCO2 at these locations. Regarding to monthly fCO2 observations, the model also well simulates the fCO2 distribution and its temporal variations along a track located between 20 ° and 50 °S with a maximal error of + 10 μatm. The model is also used to predict fCO2 for 2 ° × 2 ° grids over the entire Indian Ocean and simulates seasonal cycles that are consistent with observations. The monthly fCO2 fields derived from the model are used to estimate a global air-sea CO2 flux over the Indian Ocean basin. We estimate a net sink of 0.5 Gt/yr C for the Indian Ocean (20 °N-50 °S), with the main sink located between 20 ° and 50 °S.  相似文献   

7.
The South China Sea (SCS) exhibits strong variations on seasonal to interannual time scale, and the changing Southeast Asian Monsoon has direct impacts on the nutrients and phytoplankton dynamics, as well as the carbon cycle. A Pacific basin-wide physical-biogeochemical model has been developed and used to investigate the physical variations, ecosystem responses, and carbon cycle consequences. The Pacific basin-wide circulation model, based on the Regional Ocean Model Systems (ROMS) with a 50-km spatial resolution, is driven with daily air-sea fluxes derived from the National Centers for Environmental Prediction (NCEP) reanalysis between 1990 and 2004. The biogeochemical processes are simulated with the Carbon, Si(OH)4, Nitrogen Ecosystem (CoSINE) model consisting of multiple nutrients and plankton functional groups and detailed carbon cycle dynamics. The ROMS-CoSINE model is capable of reproducing many observed features and their variability over the same period at the SouthEast Asian Time-series Study (SEATS) station in the SCS. The integrated air-sea CO2 flux over the entire SCS reveals a strong seasonal cycle, serving as a source of CO2 to the atmosphere in spring, summer and autumn, but acting as a sink of CO2 for the atmosphere in winter. The annual mean sea-to-air CO2 flux averaged over the entire SCS is +0.33 moles CO2 m−2year−1, which indicates that the SCS is a weak source of CO2 to the atmosphere. Temperature has a stronger influence on the seasonal variation of pCO2 than biological activity, and is thus the dominant factor controlling the oceanic pCO2 in the SCS. The water temperature, seasonal upwelling and Kuroshio intrusion determine the pCO2 differences at coast of Vietnam and the northwestern region of the Luzon Island. The inverse relationship between the interannual variability of Chl-a in summer near the coast of Vietnam and NINO3 SST (Sea Surface Temperature) index in January implies that the carbon cycle and primary productivity in the SCS is teleconnected to the Pacific-East Asian large-scale climatic variability.  相似文献   

8.
The seasonal variability of the carbon dioxide (CO2) system in the Southern Ocean, south of 50°S, is analysed from observations obtained in January and August 2000 during OISO cruises conducted in the Indian Antarctic sector. In the seasonal ice zone, SIZ (south of 58°S), surface ocean CO2 concentrations are well below equilibrium during austral summer. During this season, when sea-ice is not obstructing gas exchange at the air–sea interface, the oceanic CO2 sink ranges from −2 to −4 mmol/m2/d in the SIZ. In the permanent open ocean zone, POOZ (50–58°S), surface oceanic fugacity fCO2 increases from summer to winter. The seasonal fCO2 variations (from 10 to 30 μatm) are relatively low compared to seasonal amplitudes observed in the subtropics or the subantarctic zones. However, these variations in the POOZ are large enough to cross the atmospheric level from summer to winter. Therefore, this region is neither a permanent CO2 sink nor a permanent CO2 source. In the POOZ, air–sea CO2 fluxes calculated from observations are about −1.1 mmol/m2/d in January (a small sink) and 2.5 mmol/m2/d in August (a source). These estimates obtained for only two periods of the year need to be extrapolated on a monthly scale in order to calculate an integrated air–sea CO2 flux on an annual basis. For doing this, we use a biogeochemical model that creates annual cycles for nitrate, inorganic carbon, total alkalinity and fCO2. The changing pattern of ocean CO2 summer sink and winter source is well reproduced by the model. It is controlled mainly by the balance between summer primary production and winter deep vertical mixing. In the POOZ, the annual air–sea CO2 flux is about −0.5 mol/m2/yr, which is small compared to previous estimates based on oceanic observations but comparable to the small CO2 sink deduced from atmospheric inverse methods. For reducing the uncertainties attached to the global ocean CO2 sink south of the Polar Front the regional results presented here should be synthetized with historical and new observations, especially during winter, in other sectors of the Southern Ocean.  相似文献   

9.
The ‘International Intercomparison Exercise of fCO2 Systems’ was carried out in 1996 during the R/V Meteor Cruise 36/1 from Bermuda/UK to Gran Canaria/Spain. Nine groups from six countries (Australia, Denmark, France, Germany, Japan, USA) participated in this exercise, bringing together 15 participants with seven underway fugacity of carbon dioxide (fCO2) systems, one discrete fCO2 system, and two underway pH systems, as well as systems for discrete measurement of total alkalinity and total dissolved inorganic carbon. Here, we compare surface seawater fCO2 measured synchronously by all participating instruments. A common infrastructure (seawater and calibration gas supply), different quality checks (performance of calibration procedures for CO2, temperature measurements) and a common procedure for calculation of final fCO2 were provided to reduce the largest possible amount of controllable sources of error. The results show that under such conditions underway measurements of the fCO2 in surface seawater and overlying air can be made to a high degree of agreement (±1 μatm) with a variety of possible equilibrator and system designs. Also, discrete fCO2 measurements can be made in good agreement (±3 μatm) with underway fCO2 data sets. However, even well-designed systems, which are operated without any obvious sign of malfunction, can show significant differences of the order of 10 μatm. Based on our results, no “best choice” for the type of the equilibrator nor specifics on its dimensions and flow rates of seawater and air can be made in regard to the achievable accuracy of the fCO2 system. Measurements of equilibrator temperature do not seem to be made with the required accuracy resulting in significant errors in fCO2 results. Calculation of fCO2 from high-quality total dissolved inorganic carbon (CT) and total alkalinity (AT) measurements does not yield results comparable in accuracy and precision to fCO2 measurements.  相似文献   

10.
The seasonal and interannual variability of the air–sea CO2 flux (F) in the Atlantic sector of the Barents Sea have been investigated. Data for seawater fugacity of CO2 (fCO2sw) acquired during five cruises in the region were used to identify and validate an empirical procedure to compute fCO2sw from phosphate (PO4), seawater temperature (T), and salinity (S). This procedure was then applied to time series data of T, S, and PO4 collected in the Barents Sea Opening during the period 1990–1999, and the resulting fCO2sw estimates were combined with data for the atmospheric mole fraction of CO2, sea level pressure, and wind speed to evaluate F.The results show that the Atlantic sector of the Barents Sea is an annual sink of atmospheric CO2. The monthly mean uptake increases nearly monotonically from 0.101 mol C m− 2 in midwinter to 0.656 mol C m− 2 in midfall before it gradually decreases to the winter value. Interannual variability in the monthly mean flux was evaluated for the winter, summer, and fall seasons and was found to be ± 0.071 mol C m− 2 month− 1. The variability is controlled mainly through combined variation of fCO2sw and wind speed. The annual mean uptake of atmospheric CO2 in the region was estimated to 4.27 ± 0.68 mol C m− 2.  相似文献   

11.
The ocean is an important sink for carbon and heat, yet high-resolution measurements of biogeochemical properties relevant to global climate change are being made only sporadically in the ocean at present. There is a growing need for automated, real-time, long-term measurements of CO2 in the ocean using a network of sensors, strategically placed on ships, moorings, free-drifting buoys and autonomous remotely operated vehicles. The ground-truthing of new sensor technologies is a vital component of present and future efforts to monitor changes in the ocean carbon cycle and air–sea exchange of CO2.A comparison of a moored Carbon Interface Ocean Atmosphere (CARIOCA) buoy and shipboard fugacity of CO2 (fCO2) measurements was conducted in the western North Atlantic during two extended periods (>1 month) in 1997. The CARIOCA buoy was deployed on the Bermuda Testbed Mooring (BTM), which is located 5 km north of the site of the US Joint Global Ocean Flux Study (JGOFS) Bermuda Atlantic Time-series Study (BATS). The high frequency of sampling revealed that temperature and fCO2 responded to physical forcing by the atmosphere on timescales from diurnal to 4–8 days. Concurrent with the deployments of the CARIOCA buoy, frequent measurements of surface fCO2 were made from the R/V Weatherbird II during opportunistic visits to the BTM and BATS sites, providing a direct calibration of the CARIOCA buoy fCO2 data. Although, the in situ ground-truthing of the CARIOCA buoy was complicated by diurnal processes, sub-mesoscale and fine-scale variability, the CARIOCA buoy fCO2 data was accurate within 3±6 μatm of shipboard fCO2 data for periods up to 50 days. Longer-term assessments were not possible due to the CARIOCA buoy breaking free of the BTM and drifting into waters with different fCO2-temperature properties. Strategies are put forward for future calibration of other in situ sensors.  相似文献   

12.
Marginal seas play important roles in regulating the global carbon budget, but there are great uncertainties in estimating carbon sources and sinks in the continental margins. A Pacific basin-wide physical-biogeochemical model is used to estimate primary productivity and air-sea CO_2 flux in the South China Sea(SCS), the East China Sea(ECS), and the Yellow Sea(YS). The model is forced with daily air-sea fluxes which are derived from the NCEP2 reanalysis from 1982 to 2005. During the period of time, the modeled monthly-mean air-sea CO_2 fluxes in these three marginal seas altered from an atmospheric carbon sink in winter to a source in summer. On annualmean basis, the SCS acts as a source of carbon to the atmosphere(16 Tg/a, calculated by carbon, released to the atmosphere), and the ECS and the YS are sinks for atmospheric carbon(–6.73 Tg/a and –5.23 Tg/a, respectively,absorbed by the ocean). The model results suggest that the sea surface temperature(SST) controls the spatial and temporal variations of the oceanic pCO_2 in the SCS and ECS, and biological removal of carbon plays a compensating role in modulating the variability of the oceanic pCO_2 and determining its strength in each sea,especially in the ECS and the SCS. However, the biological activity is the dominating factor for controlling the oceanic pCO_2 in the YS. The modeled depth-integrated primary production(IPP) over the euphotic zone shows seasonal variation features with annual-mean values of 293, 297, and 315 mg/(m~2·d) in the SCS, the ECS, and the YS, respectively. The model-integrated annual-mean new production(uptake of nitrate) values, as in carbon units, are 103, 109, and 139 mg/(m~2·d), which yield the f-ratios of 0.35, 0.37, and 0.45 for the SCS, the ECS, and the YS, respectively. Compared to the productivity in the ECS and the YS, the seasonal variation of biological productivity in the SCS is rather weak. The atmospheric pCO_2 increases from 1982 to 2005, which is consistent with the anthropogenic CO_2 input to the atmosphere. The oceanic pCO_2 increases in responses to the atmospheric pCO_2 that drives air-sea CO_2 flux in the model. The modeled increase rate of oceanic pCO_2 is0.91 μatm/a in the YS, 1.04 μatm/a in the ECS, and 1.66 μatm/a in the SCS, respectively.  相似文献   

13.
Gridded fields of sea surface temperature (SST), sea level pressure (SLP), and wind speed were used in combination with data for the atmospheric mole fraction of CO2 and an empirical relationship between measured values of the fugacity of carbon dioxide in surface water and SST, to calculate the air–sea CO2 flux in the northern North Atlantic. The flux was calculated for each of the months October–March, in the time period 1981 until 2001, allowing for an assessment of the interannual variations in the region. Locally and on a monthly time scale, the interannual variability of the flux could be as high as ±100% in regions seasonally covered by sea ice. However, in open-ocean areas the variability was normally between ±20% and ±40%. The interannual variability was found to be approximately halved when fluxes averaged over each winter season were compared. Summarised over the whole northern North Atlantic, the air to sea carbon flux over winter totalled 0.08 Gton, with an interannual variability of about ±7%. On a monthly basis the interannual variations were slightly higher, about ±8% to ±13%. Changes in wind speed and atmospheric fCO2 (the latter directly related to SLP variations) accounted for most of the interannual variations of the computed air–sea CO2 fluxes. A tendency for increasing CO2 flux into the ocean with increasing values of the NAO index was identified.  相似文献   

14.
In the east of China's seas, there is a wide range of the continental shelf. The nutrient cycle and the carbon cycle in the east of China's seas exhibit a strong variability on seasonal to decadal time scales. On the basis of a regional ocean modeling system(ROMS), a three dimensional physical-biogeochemical model including the carbon cycle with the resolution(1/12)°×(1/12)° is established to investigate the physical variations, ecosystem responses and carbon cycle consequences in the east of China's seas. The ROMS-Nutrient Phytoplankton Zooplankton Detritus(NPZD) model is driven by daily air-sea fluxes(wind stress, long wave radiation, short wave radiation, sensible heat and latent heat, freshwater fluxes) that derived from the National Centers for Environmental Prediction(NCEP) reanalysis2 from 1982 to 2005. The coupled model is capable of reproducing the observed seasonal variation characteristics over the same period in the East China Sea. The integrated air-sea CO_2 flux over the entire east of China's seas reveals a strong seasonal cycle, functioning as a source of CO_2 to the atmosphere from June to October, while serving as a sink of CO_2 to the atmosphere in the other months. The 24 a mean value of airsea CO_2 flux over the entire east of China's seas is about 1.06 mol/(m~2·a), which is equivalent to a regional total of3.22 Mt/a, indicating that in the east of China's seas there is a sink of CO_2 to the atmosphere. The partial pressure of carbon dioxide in sea water in the east of China's seas has an increasing rate of 1.15 μatm/a(1μtm/a=0.101 325Pa), but p H in sea water has an opposite tendency, which decreases with a rate of 0.001 3 a~(–1) from 1982 to 2005.Biological activity is a dominant factor that controls the pCO_2 air in the east of China's seas, and followed by a temperature. The inverse relationship between the interannual variability of air-sea CO_2 flux averaged from the domain area and Ni?o3 SST Index indicates that the carbon cycle in the east of China's seas has a high correlation with El Ni?o-Southern Oscillation(ENSO).  相似文献   

15.
Factors controlling the CO2 system parameters, including the partial pressure of CO2 (PCO2) in coral reef waters, were investigated in three mid-oceanic reefs of the Indo-Pacific region. Surface water PCO2 in the lagoons of Majuro Atoll and Palau barrier reef in the Pacific were 25 µatm and 48 µatm higher than those of the offshore waters, respectively, while South Male Atoll lagoon of the Maldives in the Indian Ocean exhibited relatively small difference in PCO2 compared to the offshore water. Observations from Majuro Atoll and Palau barrier reef are consistent with the view that calcium carbonate production predominates in coral reefs. On the other hand, results from South Male Atoll can be attributed to the thorough flushing of the lagoon, which is connected to the open ocean by numerous deep channels. The offshore-lagoon PCO2 difference depends on system-level net organic-to-inorganic carbon production ratio while reef topography, especially residence time of the lagoon, has a secondary effect on the magnitude of the offshore-lagoon difference. A potential for releasing CO2 might be more evident in an enclosed atoll where the reef water has a longer residence time. Oceanic atoll and barrier reef lagoons, which are in the terminal stage of evolutionary history of oceanic volcanic islands, have the potential to release CO2 to the atmosphere.  相似文献   

16.
This study investigated the tidal asymmetry imposed by both the interaction of principal tides and the higher harmonics generated by distortions within a tidal creek network with mixed mainly semidiurnal tide in the Bushehr Port, Persian Gulf. Since velocity and water-level imposed by principal triad tides K1-O1-M2 are in quadrature, duration asymmetries during a tidal period in this short, shallow inverse estuary should be manifest as skewed velocities. The principal tides produce periodic asymmetries including a strong ebb-dominance and a weak flood-dominance condition during spring and neap tides respectively. The higher harmonics induced by nonlinearities engender a flood-dominance condition where the convergence effects are higher than frictional effects, and an ebbdominance condition where intertidal storage are extended. Since the triad K1-O1-M2 driven asymmetry is not overcome by higher harmonics close to the mouth, the periodic asymmetry dominates within the creek in which higher harmonics reinforce the weak flood-dominance (strong ebb-dominance) condition in the convergent channel (divergent area). Also, the maximum flood and the maximum ebb from all harmonic constituents occurred close to high water slack time during both spring and neap tides in this short creek. Since occational wetting of intertidal areas happened close to the high water (HW) time during spring tide, the water level flooded slowly close to the HW time of the spring tide.  相似文献   

17.
We observed the partial pressure of oceanic CO2, pCO2 sea, and related surface properties in the westernmost region of the subarctic North Pacific, seasonally from 1998 to 2001. The pCO2 sea in the Oyashio region showed a large decrease from winter to spring. In winter, pCO2 sea was higher than 400 μatm in the Oyashio region and this region was a source of atmospheric CO2. In spring, pCO2 sea decreased to extremely low values, less than 200 μatm (minimum, 139 μatm in 2001), around the Oyashio region with low surface salinity and this region turned out to be a strong sink. The spatial variations of pCO2 sea were especially large in spring in this region. The typical Oyashio water with minimal mixing with subtropical warm water was extracted based on the criterion of potential alkalinity. The contribution of main oceanic processes to the changes in pCO2 sea from winter to spring was estimated from the changes in the concentrations of dissolved inorganic carbon and nutrients, total alkalinity, temperature and salinity observed in surface waters in respective years. These quantifications indicated that photosynthesis made the largest contribution to the observed pCO2 sea decreases in all years and its magnitude was variable year by year. These year-to-year differences in spring biological contribution could be linked to those in the development of the density stratification due to the decrease in surface salinity. Thus, the changes in the surface physical structure could induce those in pCO2 sea in the Oyashio region in spring. Furthermore, it is suggested that the direction and magnitude of the air-sea CO2 flux during this season could be controlled significantly by the onset time of the spring bloom. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

18.
The interannual variations of CO2 sources and sinks in the surface waters of the Antarctic Ocean (south of 50°S) were studied between 1986 and 1994. An existing, slightly modified one-dimensional model describing the mixed-layer carbon cycle was used for this study and forced by available satellite-derived and climatological data. Between 1986 and 1994, the mean Antarctic Ocean CO2 uptake was 0.53 Pg C year−1 with an interannual variability of 0.15 Pg C year−1.Interannual variation of the Antarctic Ocean CO2 uptake is related to the Antarctic Circumpolar Wave (ACW), which affects sea surface temperature (SST), wind-speed and sea-ice extent. The CO2 uptake in the Antarctic Ocean has increased from 1986 to 1994 by 0.32 Pg C. It was found that over the 9 years, the surface ocean carbon dioxide fugacity (fCO2) increase was half that of the atmospheric CO2 increase inducing an increase of the air–sea fCO2 gradient. This effect is responsible for 60% of the Antarctic Ocean CO2 uptake increase between 1986 and 1994, as the ACW effect cancels out over the 9 years investigated.  相似文献   

19.
pH and alkalinity measurements from a coastal upwelling area located near 30°S (Coquimbo, Chile), are used to describe the short-term variations of CO2 air–sea exchanges over a period of one week in summer 1996. A 180 km ocean–coastal transect, together with two almost-synoptic grid surveys off Coquimbo covering approximate 2500 km2 each, showed that during and immediately after a 4 day long southwesterly wind event (24–28 January) a large area of cold surface water (≈14°C), highly supersaturated in CO2 (fCO2 up to 900 μatm), was located near the coast. Three days after the end of the event, the second grid survey showed that in most of the study area the surface temperature and pH had increased significantly (by 1–3°C and 0.05–0.2, respectively), and that the surface water was no longer supersaturated in CO2. The CO2-supersaturated water observed in the first grid survey was identified as upwelled subsurface equatorial water, a water mass with its core at about 200 m depth: the depth from which the water upwells is a major determinant of the surface water fCO2. Integrated C fluxes within a 20 km wide coastal strip (1900 km2) indicate a strong outgassing of CO2 from the ocean under upwelling conditions (Grid 1; 121 t C day-1), while the net C exchange was directed to the ocean during the relaxation period (Grid 2; 19 t C day-1). Estimates of CO2 fluxes in upwelling areas based on surface water fCO2 measurements must therefore take into account these short-term variations: reliance on longer-term averages and interpolation will lead to erroneous results.  相似文献   

20.
Intense studies of upper and deep ocean processes were carried out in the Northwestern Indian Ocean (Arabian Sea) within the framework of JGOFS and related projects in order to improve our understanding of the marine carbon cycle and the ocean’s role as a reservoir for atmospheric CO2. The results show a pronounced monsoon-driven seasonality with enhanced organic carbon fluxes into the deep-sea during the SW Monsoon and during the early and late NE Monsoon north of 10°N. The productivity is mainly regulated by inputs of nutrients from subsurface waters into the euphotic zone via upwelling and mixed layer-deepening. Deep mixing introduces light limitation by carrying photoautotrophic organisms below the euphotic zone during the peak of the NE Monsoon. Nevertheless, deep mixing and strong upwelling during the SW Monsoon provide an ecological advantage for diatoms over other photoautotrophic organisms by increasing the silica concentrations in the euphotic zone. When silica concentrations fall below 2 μmol l−1, diatoms lose their dominance in the plankton community. During diatom-dominated blooms, the biological pathway of uptake of CO2 (the biological pump) appears to be more efficient than during blooms of other organisms, as indicated by organic carbon to carbonate carbon (rain) ratios. Due to the seasonal alternation of diatom and non-diatom dominated exports, spatial variations of the annual mean rain ratios are hardly discernible along the main JGOFS transect.Data-based estimates of the annual mean impact of the biological pump on the fCO2 in the surface water suggest that the biological pump reduces the increase of fCO2 in the surface water caused by intrusion of CO2-enriched subsurface water by 50–70%. The remaining 30 to 50% are attributed to CO2 emissions into the atmosphere. Rain ratios up to 60% higher in river-influenced areas off Pakistan and in the Bay of Bengal than in the open Arabian Sea imply that riverine silica inputs can further enhance the impact of the biological pump on the fCO2 in the surface water by supporting diatom blooms. Consequently, it is assumed that reduced river discharges caused by the damming of major rivers increase CO2 emission by lowering silica inputs to the Arabian Sea; this mechanism probably operates in other regions of the world ocean also.  相似文献   

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